Enhanced Recovery After Major Surgery and Chronic Pain for Total Knee Arthroplasty
NCT: NCT05981105 · ACTIVE_NOT_RECRUITING
Brief Summary
The goal of this interventional clinical trial is to assess opioid consumption 24-48 hrs post anesthesia block among patients undergoing total knee arthroplasty. The main question it aims to answer is: 1\. Is there a difference in opioid consumption 24-48 hours post block administration among patients that receive an adductor canal catheter (ACC) versus adductor canal block (ACB)? Participants will be: * Randomized to receive an adductor canal catheter (ACC) or a sham adductor canal catheter. * Asked to use the Diagnotes application to communicate with the pain doctor while the catheter is in place. * Follow up for up to 6 months post-operation. Researchers will compare the interventional group (ACC) to the control group (sham ACC + ACB) to see if there is difference in opioid consumption and chronic pain at 6 months post-operation.
Frequently Asked Questions
What is Enhanced Recovery After Major Surgery and Chronic Pain for Total Knee Arthroplasty?
Enhanced Recovery After Major Surgery and Chronic Pain for Total Knee Arthroplasty is a clinical trial registered under NCT05981105. Current status: ACTIVE_NOT_RECRUITING.
What is the status of NCT05981105?
The current status of NCT05981105 (Enhanced Recovery After Major Surgery and Chronic Pain for Total Knee Arthroplasty) is: ACTIVE_NOT_RECRUITING.
When did Enhanced Recovery After Major Surgery and Chronic Pain for Total Knee Arthroplasty start?
Enhanced Recovery After Major Surgery and Chronic Pain for Total Knee Arthroplasty started on 2023-06-12.
Related Devices
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.